Agathe Subtil

4.4k total citations · 1 hit paper
59 papers, 3.3k citations indexed

About

Agathe Subtil is a scholar working on Microbiology, Molecular Biology and Epidemiology. According to data from OpenAlex, Agathe Subtil has authored 59 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Microbiology, 24 papers in Molecular Biology and 17 papers in Epidemiology. Recurrent topics in Agathe Subtil's work include Reproductive tract infections research (31 papers), Cellular transport and secretion (14 papers) and Urinary Tract Infections Management (12 papers). Agathe Subtil is often cited by papers focused on Reproductive tract infections research (31 papers), Cellular transport and secretion (14 papers) and Urinary Tract Infections Management (12 papers). Agathe Subtil collaborates with scholars based in France, United States and Germany. Agathe Subtil's co-authors include Alice Dautry‐Varsat, Timothy E. McGraw, Michael A. Lampson, Stéphanie Perrinet, Keith Kobylarz, James H. Keen, Ibragim Gaidarov, Agnès Hémar, Cédric Delevoye and Pierre Dehoux and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Cell Biology.

In The Last Decade

Agathe Subtil

57 papers receiving 3.3k citations

Hit Papers

Acute cholesterol depletion inhibits clathrin-coated pit ... 1999 2026 2008 2017 1999 100 200 300 400 500

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Agathe Subtil France 34 1.6k 1.0k 704 666 666 59 3.3k
Johannes H. Hegemann Germany 34 2.5k 1.5× 764 0.7× 790 1.1× 536 0.8× 323 0.5× 98 3.7k
M. S. Blake United States 30 1.7k 1.0× 1.3k 1.2× 239 0.3× 604 0.9× 622 0.9× 50 3.9k
Yasuhiko Horiguchi Japan 30 1.7k 1.1× 481 0.5× 317 0.5× 316 0.5× 473 0.7× 98 3.4k
Morgane Bomsel France 41 1.9k 1.2× 301 0.3× 889 1.3× 833 1.3× 1.7k 2.6× 108 5.3k
Drusilla Burns United States 32 1.4k 0.8× 1.0k 1.0× 230 0.3× 613 0.9× 435 0.7× 94 3.0k
Ronald S. Flannagan Canada 27 1.9k 1.2× 235 0.2× 293 0.4× 461 0.7× 979 1.5× 51 4.0k
Knut Adermann Germany 34 1.9k 1.1× 1.1k 1.0× 139 0.2× 174 0.3× 898 1.3× 86 3.6k
Alex Bollen Belgium 40 2.5k 1.5× 279 0.3× 316 0.4× 929 1.4× 1.2k 1.8× 192 5.5k
David G. Klapper United States 35 1.5k 0.9× 496 0.5× 158 0.2× 261 0.4× 600 0.9× 82 3.6k
Florence Niedergang France 35 969 0.6× 155 0.2× 589 0.8× 282 0.4× 1.3k 2.0× 75 3.0k

Countries citing papers authored by Agathe Subtil

Since Specialization
Citations

This map shows the geographic impact of Agathe Subtil's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Agathe Subtil with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Agathe Subtil more than expected).

Fields of papers citing papers by Agathe Subtil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Agathe Subtil. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Agathe Subtil. The network helps show where Agathe Subtil may publish in the future.

Co-authorship network of co-authors of Agathe Subtil

This figure shows the co-authorship network connecting the top 25 collaborators of Agathe Subtil. A scholar is included among the top collaborators of Agathe Subtil based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Agathe Subtil. Agathe Subtil is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Cicco, Aurélie Di, Tal Keren‐Kaplan, Sílvia Vale-Costa, et al.. (2022). PI4P and BLOC-1 remodel endosomal membranes into tubules. The Journal of Cell Biology. 221(11). 16 indexed citations
2.
Triboulet, Sébastien, et al.. (2022). CT295 Is Chlamydia trachomatis’ Phosphoglucomutase and a Type 3 Secretion Substrate. Frontiers in Cellular and Infection Microbiology. 12. 866729–866729. 4 indexed citations
3.
Liu, Chang, Henri Cohen, Aminata Kane, et al.. (2021). Primary ectocervical epithelial cells display lower permissivity to Chlamydia trachomatis than HeLa cells and a globally higher pro-inflammatory profile. Scientific Reports. 11(1). 5848–5848. 6 indexed citations
4.
Lystad, Alf Håkon, et al.. (2020). The Chlamydia effector CT622/TaiP targets a nonautophagy related function of ATG16L1. Proceedings of the National Academy of Sciences. 117(43). 26784–26794. 13 indexed citations
5.
Francetić, Olivera, et al.. (2017). Tracking Proteins Secreted by Bacteria: What's in the Toolbox?. Frontiers in Cellular and Infection Microbiology. 7. 221–221. 48 indexed citations
6.
Cenci, Ugo, Debashish Bhattacharya, Andreas P.M. Weber, et al.. (2017). Biotic Host–Pathogen Interactions As Major Drivers of Plastid Endosymbiosis. Trends in Plant Science. 22(4). 316–328. 32 indexed citations
7.
Perrinet, Stéphanie, et al.. (2016). The DUF582 Proteins of Chlamydia trachomatis Bind to Components of the ESCRT Machinery, Which Is Dispensable for Bacterial Growth In vitro. Frontiers in Cellular and Infection Microbiology. 6. 123–123. 19 indexed citations
8.
Hayward, Richard D., et al.. (2016). One Face of Chlamydia trachomatis: The Infectious Elementary Body. Current topics in microbiology and immunology. 412. 35–58. 24 indexed citations
9.
Perrinet, Stéphanie, et al.. (2014). Quantitative Monitoring of the Chlamydia trachomatis Developmental Cycle Using GFP-Expressing Bacteria, Microscopy and Flow Cytometry. PLoS ONE. 9(6). e99197–e99197. 36 indexed citations
10.
Ball, Steven, Agathe Subtil, Debashish Bhattacharya, et al.. (2013). Metabolic Effectors Secreted by Bacterial Pathogens: Essential Facilitators of Plastid Endosymbiosis? . The Plant Cell. 25(1). 7–21. 74 indexed citations
11.
Bierne, Hélène, Laetitia Travier, Tanel Mahlakõiv, et al.. (2012). Activation of Type III Interferon Genes by Pathogenic Bacteria in Infected Epithelial Cells and Mouse Placenta. PLoS ONE. 7(6). e39080–e39080. 80 indexed citations
12.
Dehoux, Pierre, Rhonda Flores, Catherine Dauga, Guangming Zhong, & Agathe Subtil. (2011). Multi-genome identification and characterization of chlamydiae-specific type III secretion substrates: the Inc proteins. BMC Genomics. 12(1). 109–109. 98 indexed citations
13.
Pennini, Meghan E., Stéphanie Perrinet, Alice Dautry‐Varsat, & Agathe Subtil. (2010). Histone Methylation by NUE, a Novel Nuclear Effector of the Intracellular Pathogen Chlamydia trachomatis. PLoS Pathogens. 6(7). e1000995–e1000995. 131 indexed citations
14.
Paumet, Fabienne, Jordan Wesolowski, Alejandro Garcia-Diaz, et al.. (2009). Intracellular Bacteria Encode Inhibitory SNARE-Like Proteins. PLoS ONE. 4(10). e7375–e7375. 74 indexed citations
15.
Balañá, María Eugenia, Florence Niedergang, Agathe Subtil, et al.. (2005). ARF6 GTPase controls bacterial invasion by actin remodelling. Journal of Cell Science. 118(10). 2201–2210. 55 indexed citations
16.
Dautry‐Varsat, Alice, Agathe Subtil, & Ted Hackstadt. (2005). Recent insights into the mechanisms of Chlamydia entry. Cellular Microbiology. 0(0). 127739821–???. 87 indexed citations
17.
Subtil, Agathe, et al.. (2005). A directed screen for chlamydial proteins secreted by a type III mechanism identifies a translocated protein and numerous other new candidates. Molecular Microbiology. 56(6). 1636–1647. 113 indexed citations
18.
Subtil, Agathe, Claude Parsot, & Alice Dautry‐Varsat. (2001). Secretion of predicted Inc proteins of Chlamydia pneumoniae by a heterologous type III machinery. Molecular Microbiology. 39(3). 792–800. 134 indexed citations
19.
Subtil, Agathe, Muriel Delepierre, & Alice Dautry‐Varsat. (1997). An α-Helical Signal in the Cytosolic Domain of the Interleukin 2 Receptor β Chain Mediates Sorting Towards Degradation after Endocytosis. The Journal of Cell Biology. 136(3). 583–595. 46 indexed citations
20.
Hémar, Agnès, Michèle Lieb, Agathe Subtil, James P. Di Santo, & Alice Dautry‐Varsat. (1994). Endocytosis of the β chain of interleukin‐2 receptor requires neither interleukin‐2 nor the γ chain. European Journal of Immunology. 24(9). 1951–1955. 22 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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